World's Best Scientists 2026 revealed!
Min-Xin Guan

Min-Xin Guan

D-Index & Metrics

Genetics

D-Index
66
Citations
13831
World Ranking
2633
National Ranking
70

Min-Xin Guan publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Min-Xin Guan sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 315 publications — 78th percentile

78% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Min-Xin Guan D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Min-Xin Guan sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 66 D-Index — 41st percentile

41% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Min-Xin Guan is affiliated with Zhejiang University in China and specializes in Biochemistry, Genetics and Molecular Biology with a total of 127 publications in this field. Their research interest is strongly focused on Molecular Biology, which accounts for 110 of their works, along with contributions to Clinical Biochemistry, Sensory Systems, Cancer Research, and Neurology.

The scientist's main topics of study include:

  • Mitochondrial Function and Pathology
  • ATP Synthase and ATPases Research
  • RNA modifications and cancer
  • RNA and protein synthesis mechanisms
  • Metabolism and Genetic Disorders
  • Hearing, Cochlea, Tinnitus, Genetics
  • RNA Research and Splicing

Min-Xin Guan has published in several prominent journals multiple times. Frequent publication venues encompass:

  • Journal of Biological Chemistry (10 publications)
  • Nucleic Acids Research (6 publications)
  • JCI Insight (4 publications)
  • Human Molecular Genetics (4 publications)
  • PubMed (4 publications)

Recent papers authored or co-authored by Min-Xin Guan include:

  • ATAD3B is a mitophagy receptor mediating clearance of oxidative stress-induced damaged mitochondrial DNA, 2021, The EMBO Journal
  • Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAs, 2022, Nature Communications
  • Emerging functions of mitochondria-encoded noncoding RNAs, 2022, Trends in Genetics
  • PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy, 2020, Journal of Clinical Investigation
  • A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation, 2020, Nucleic Acids Research

Their network of frequent coauthors reflects collaborations with the following researchers:

  • Yanchun Ji (17 collaborations)
  • Feilong Meng (14 collaborations)
  • Juanjuan Zhang (13 collaborations)
  • Meng Wang (9 collaborations)
  • Qiuzi Yi (9 collaborations)

Overall, Min-Xin Guan's scientific contributions cover diverse aspects of mitochondrial biology, RNA processes, and genetic mechanisms related to metabolism and sensory systems, supported by extensive publication activity in leading journals and active collaborative research.

Best Publications

  • DarkSide-20k: A 20 tonne two-phase LAr TPC for direct dark matter detection at LNGS

    C. E. Aalseth;F. Acerbi;P. Agnes;I. F. M. Albuquerque

  • Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

    Hui Zhao;Ronghua Li;Qiuju Wang;Qingfeng Yan

  • Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

    Zhiyuan Li;Ronghua Li;Jianfu Chen;Zhisu Liao

  • Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

    Min-Xin Guan;Min-Xin Guan;Qingfeng Yan;Xiaoming Li;Yelena Bykhovskaya

  • The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells

    Qianqian Li;Zewen Gao;Ye Chen;Min-Xin Guan

  • A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Species identification through mitochondrial rRNA genetic analysis

    Li Yang;Zongqing Tan;Daren Wang;Ling Xue

  • Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness.

    Nuno Raimundo;Lei Song;Timothy E. Shutt;Sharen E. McKay

  • Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss.

    Ronghua Li;Guangqian Xing;Ming Yan;Xing Cao

  • Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

    Min-Xin Guan

  • The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNASer(UCN) Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression

    Min-Xin Guan;José Antonio Enriquez;Nathan Fischel-Ghodsian;Ram S. Puranam

  • Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNALeu(UUR) A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Symptoms and Diabetes

    Ronghua Li;Min-Xin Guan;Min-Xin Guan

  • Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation

    Xiaoming Li;Ronghua Li;Xinhua Lin;Min-Xin Guan

  • Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness

    Xiaoming Li;Nathan Fischel‐Ghodsian;Faina Schwartz;Qingfeng Yan

  • The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.

    Jia Qu;Ronghua Li;Xiangtian Zhou;Yi Tong

  • Molecular pathogenetic mechanism of maternally inherited deafness.

    Min-Xin Guan

  • Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

    Jianxin Lu;Zhiyuan Li;Yi Zhu;Aifen Yang

  • Prevalence of Mitochondrial 12S rRNA Mutations Associated with Aminoglycoside Ototoxicity.

    Min-Xin Guan

Frequent Co-Authors

Jia Qu
Jia Qu Wenzhou Medical University
J. Napolitano
J. Napolitano Temple University

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